等级
certified reference material
特点
Snap-N-Spike®/Snap-N-Shoot®
包装
ampule of 1.2 mL
制造商/商品名称
Cerilliant®
浓度
100 μg/mL in H2O
格式
single component solution
储存温度
2-8°C
SMILES字符串
NCP(O)(O)=O
InChI
1S/CH6NO3P/c2-1-6(3,4)5/h1-2H2,(H2,3,4,5)
InChI key
MGRVRXRGTBOSHW-UHFFFAOYSA-N
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法律信息
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Fabrizio Botta et al.
Chemosphere, 77(1), 133-139 (2009-06-02)
A study of glyphosate and aminomethyl phosphonic acid (AMPA) transfer in the Orge watershed (France) was carried out during 2007 and 2008. Water samples were collected in surface water, wastewater sewer, storm sewer and wastewater treatment plant (WWTP). These two
A S F Araújo et al.
Chemosphere, 52(5), 799-804 (2003-05-22)
Glyphosate [N-(phosphonomethyl)-glycine] is a broad-spectrum, non-selective, post-emergence herbicide that is widely used in agricultural. We studied, in vitro, changes in the microbial activity of typical Hapludult and Hapludox Brazilian soils, with and without applied glyphosate. Glyphosate was applied at a
M J Shaw et al.
Journal of chromatography. A, 876(1-2), 127-133 (2000-05-24)
High-performance chelation ion chromatography (HPCIC), involving a chelating silica substrate bonded with aminomethylphosphonic acid, has been developed as a novel technique for the quantitative determination of beryllium in complex matrices. An isocratic separation method, using an eluent containing 1 M
Residues of glyphosate and its principle metabolite in certain cereals, oilseeds, and pulses grown in Canada, 1990-1992.
Y Y Wigfield et al.
Bulletin of environmental contamination and toxicology, 53(4), 543-547 (1994-10-01)
M Tomita et al.
Journal of chromatography, 571(1-2), 324-330 (1991-11-15)
Capillary electrophoresis has been used to separate and quantitate glyphosate and its major metabolite, (aminomethyl)phosphonic acid (AMPA), in serum. The two compounds, after derivatization with p-toluenesulphonyl chloride, were clearly separated with 0.1 M boric acid-sodium hydroxide buffer (pH 9.6) containing
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